Opis stanowiska podany przez pracodawcę:

Job Tasks:

• Regulatory Affairs data entry activities (e.g. track incoming data entry requests and follow up until completion in alignment with global and regional data quality standards and procedures
• Ad hoc activities (e. g. support data owners with guidance, training, instructions on the process and requirements for maintaining data in the relevant systems
• Align with supervisor and team members to ensure data entry backup capabilities during vacation and holiday periods 
• Perform other related tasks as assigned by supervisor
• Maintain compliance with all company policies and procedures

Requirements:

• Good understanding of pharmaceutical Marketing Authorisation data and regulatory procedures (national as well as EU procedures)
• Understanding of regulatory data planning and tracking requirements
• Knowledge of compliance requirements and advanced process thinking
• Good technical skills and computer proficiency
• Proven ability to monitor multiple actions and timelines and follow up until timely completion
• Ability to work effectively in a matrix organisation with multiple cross-functional stakeholders on global, regional and local level
• Excellent cross-cultural communication skills in English

Offer: 

• Opportunity to work for a global Big Pharma company
• Stable job environment
• International team
• Benefits package
• Hybrid or remote job
• Full time remote work on a 6-12 months project with option for prolongate

The offer applies to permanent work.

Kontakt do pracodawcy:

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